Taiwan FDA registration bdca97736726f6a1c614f4d24e23dc3c
“gke” Bowie-Dick-Simulation Test
TW: “記錄易”滅菌記錄真空模擬測試裝置
Taiwan·Risk Class 2·MD·gke-GmbH·Registered Nov 01, 2016 – Nov 01, 2021ExpiredRegistration details
- Analysis ID
- bdca97736726f6a1c614f4d24e23dc3c
- License Form
- Ministry of Health Medical Device Import No. 029005
- Customs Code
- DHA05602900507
Company information
- Manufacturer
- gke-GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- Yida Industrial Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J2800 Sterilization Process Indicator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 01, 2016
- Expiry Date
- Nov 01, 2021
About this record
Access comprehensive regulatory information for “gke” Bowie-Dick-Simulation Test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bdca97736726f6a1c614f4d24e23dc3c and manufactured by gke-GmbH. The authorized representative in Taiwan is Yida Industrial Co., Ltd.
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